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FDA 510(k), K923771, PULSE RF TEST
FDA 510(k), K923771, PULSE RF TEST
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510(K) Number: K923771
Device Name: PULSE RF TEST
Manufacturer: ALLE CHAN
Device Classification Name: System, Test, Rheumatoid Factor
Regulation Number: DHR
Classification Product Code: 07/28/1992
Date Received: 10/05/1992
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Immunology
Device Name: PULSE RF TEST
Manufacturer: ALLE CHAN
Device Classification Name: System, Test, Rheumatoid Factor
Regulation Number: DHR
Classification Product Code: 07/28/1992
Date Received: 10/05/1992
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Immunology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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